Effector and regulatory lymphocytes in asthmatic pregnant women

Am J Reprod Immunol. 2010 Dec;64(6):393-401. doi: 10.1111/j.1600-0897.2010.00878.x.

Abstract

Problem: Asthma influences pregnancy outcome and pregnancy affects asthma severity, but the immunologic mechanisms of these interactions are not fully elucidated.

Method: The prevalence of lymphocyte subsets was identified by cell surface markers and intracellular FoxP3 staining, in healthy non-pregnant (HNP; N = 15), healthy pregnant (HP; N=33), asthmatic non-pregnant (ANP; N=62) and asthmatic pregnant (AP; N=61) women.

Results: Regulatory T cell (Treg) prevalence was higher in HP than in HNP subjects and showed a positive correlation with fetal birth weight, which was blunted in AP group. Treg prevalence was lower and invariable natural killer T cell prevalence was higher in AP patients (compared to HP). Higher naive and lower effector T cell prevalence was observed in AP than in ANP group.

Conclusion: Pregnancy-induced increase in Treg cell prevalence is absent in asthmatic pregnancy that may interfere with physiological intrauterine growth. However, pregnancy-specific inhibition of asthmatic inflammation can be detected in uncomplicated asthmatic pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, CD / metabolism
  • Antigens, Differentiation / metabolism
  • Asthma / immunology*
  • Asthma / physiopathology
  • Disease Progression
  • Female
  • Fetal Weight
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Immunologic Memory
  • Lymphocyte Subsets / immunology
  • Lymphocyte Subsets / metabolism*
  • Lymphocyte Subsets / pathology
  • Natural Killer T-Cells / immunology
  • Natural Killer T-Cells / metabolism*
  • Natural Killer T-Cells / pathology
  • Pregnancy
  • Pregnancy Complications / immunology*
  • Pregnancy Complications / physiopathology
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / metabolism*
  • T-Lymphocytes, Regulatory / pathology

Substances

  • Antigens, CD
  • Antigens, Differentiation
  • FOXP3 protein, human
  • Forkhead Transcription Factors